Hereditárna sférocytóza
Guidelines for the diagnosis and management of hereditary spherocytosis
P. H. B. Bolton-Maggs 1, R. F. Stevens 2, N. J. Dodd 3, G. Lamont 4, P. Tittensor5and M.-J. King 6 on behalf of the General Haematology Task Force of the British Committee for Standards in Haematology
1 Manchester Royal Infirmary, Manchester
2 Royal Manchester Children's Hospital, Manchester
3 The Ipswich Hospital NHS Trust Ipswich
4 Royal Liverpool Children's Hospital, Alder Hey, Liverpool
5 Patient Representative, and
6 International Blood Group Reference Laboratory, Bristol, UK
British Journal of Haematology 2004, 126, 455-474
Čítať ďalej
P. H. B. Bolton-Maggs 1, R. F. Stevens 2, N. J. Dodd 3, G. Lamont 4, P. Tittensor5and M.-J. King 6 on behalf of the General Haematology Task Force of the British Committee for Standards in Haematology
1 Manchester Royal Infirmary, Manchester
2 Royal Manchester Children's Hospital, Manchester
3 The Ipswich Hospital NHS Trust Ipswich
4 Royal Liverpool Children's Hospital, Alder Hey, Liverpool
5 Patient Representative, and
6 International Blood Group Reference Laboratory, Bristol, UK
British Journal of Haematology 2004, 126, 455-474